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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 653981Erstellt: 26. Oktober 2026

Chlorotrimethylsilane → HCID 15126108, Verbindung

https://huagongshe.com/reaction/653981

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
EduktHexamethyldisilazaneHCID 13838—
EduktSodium BicarbonateHCID 516892—
Edukt1-O-Acetyl-5-O-t-butyldiphenylsilyl-4-thio-2,3-dideoxyribofuranoseHCID 15126098—
EduktPotassium perfluorobutanesulfonateHCID 23675274—
EduktCytosineHCID 178418229—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 15126108HCID 15126108—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A mixture of 10 (0.26 g, 0.63 mmol), cytosine (0.105 g, 0.95 mmol), and potassium nonafluorobutanesulfonate (0.77 g, 2.3 mmol) was suspended in 12 mL dry acetonitrile under nitrogen. HMDS (0.135 mL, 0.63 mmol) and TMS-Cl (0.37 mL, 2.9 mmol) were added sequentially via syringe and the reaction stirred at 25° C. overnight. The reaction was poured into a mixture of 20 mL dichloromethane and 15 mL saturated NaHCO3 and shaken. The organic phase was dried (MgSO4) and concentrated in vacuo. The anomeric mixture was separated by preparative TLC with 7.5% MeOH/CHCl3 with an ammonia atmosphere: yield of β-anomer, 78 mg and 117 mg of the α-anomer to afford total yield of 195 mg (66.5%); FAB MS 466 (M+H)+ ; 1H NMR (CDCl3) of α/β anomer, δ 8.12 (d, 1, 6-H), 7.7 (m, 4, ArH), 7.4 (m, 6, ArH), 6.32 (m, 1, 1'-H), 5.9-5.3 (hump, 1, NH2), 5.75 (d, 1, 5-H), 5.45 (d, 1, 5-H), 3.75 (m, 3, 4'-Hα,β 's, 3'-Hα,β 's).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05128458
Quelldatensatzuspto-grants-1992_07
ORD IDord-e369a01e7e4949d5a42ef03f07094859
Quellennotizuspto-grants-1992_07